• Cancer

• 415.

Dean Snell Cancer Foundation

TO ASSIST CANCER PATIENTS WITH EXPENSES NOT COVERED BY INSURANCE OR STATE FUNDS.

• Surgery

• 416.

American Association of Neurosurgeons Inc

NREF, the philanthropic arm of @AANSNeuro, advances patient care by supporting neurosurgical research, education and innovation.

• Alliance/Advocacy Organizations

• 417.

The Cute Syndrome Foundation, Inc.

The Cute Syndrome Foundation raises awareness of SCN8A mutations, funds the dedicated and talented scientists researching SCN8A, and supports the families around the world who are affected by SCN8A-related disorders.

• Eye Diseases, Blindness & Vision Impairment

• 418.

MACULAR DEGENERATION SUPPORT INC

To provide information and support for people who are affected by macular degeneration and similar retinal diseases.

• Diseases, Disorders, Medical Disciplines N.E.C.

• 419.

Trisomy 18 Bridge of Hope Foundation Inc

Search this site Building a Better Today and Tomorrow for Children with Trisomy 18 Hope Help and Information to help you advocate for your child I want you to know that you and your child are so very special.

• Public Foundations

• 420.

The Silverstein Foundation for Gba Research

The Silverstein Foundation: Accelerating research in Parkinson's with GBA Accelerating research in Parkinsonswith GBA The Silverstein Foundation for Parkinsons with GBA supports cutting edge research with the goal of discovering new therapies for the treatment of Parkinsons Disease in glucocerebrosidase GBA mutation carriers.

LOVING EYES FOUNDATION

Committed to preventing vision loss among children by developing technology that provides the eyewear they need to thrive.

• Nonmonetary Support N.E.C.*

• 422.

Global Neuro Ycare Inc

The mission of Global Neuro YCare is to educate through the creation and translation of materials and programs for children, youth and families; advocate with national and international organizations to guide the creation of regional, cultural and country specific programming; and support research addressing the needs and experiences of young carers.

Lambert-Eaton Lems Family Association

We advocate for patients, family and caregivers who have the extremely rare neuromuscular disorder, Lambert-Eaton Myasthenic Syndrome.